Cationic nitrogen-containing heterocycles and their application in wellbore stability

ABSTRACT

In accordance with one or more embodiments of the present disclosure, a method of inhibiting shale formation during water-based drilling of subterranean formations includes introducing a shale inhibitor to the subterranean formation during the water-based drilling, the shale inhibitor comprising a cationic polymer comprising repeating units of [A-B]. A is a substituted benzene or a substituted triazine of formula (2). B is a N-containing heterocycle. The cationic polymer and a method of making the cationic polymer are also described.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a divisional application of U.S. patentapplication Ser. No. 17/004,563, filed Aug. 27, 2020, the entirecontents of which are incorporated by reference in the presentdisclosure.

FIELD

Embodiments of the present disclosure generally relate to wellborestability, and pertain particularly to cationic polymers and methods ofusing the cationic polymers for inhibiting shale formation duringwater-based drilling of subterranean formations.

TECHNICAL BACKGROUND

Drilling fluids may be added to subterranean formations for manypurposes, including suspending and transporting drill cuttings, coolingand lubricating the drilling bits, maintaining borehole stability, andreducing formation damage. In general, there are water-based drillingfluids and oil-based drilling fluids. Oil-based drilling fluids tend tobe stable under the elevated temperatures and pressures common in atleast the deeper portions of the borehole but also suffer from handlingand environmental issues. Water-based drilling fluids, although lower incost and environmental impact, may severely damage the wellbore. Severehydration and swelling of clays in the bore can narrow the borediameter, alter the stress distribution around the borehole, reduce theshale mechanical strength, and cause borehole instability. Dispersion ofclay and shale may accelerate wellbore sloughing and deteriorate therheological properties of drilling fluids. Eventually, the drillingprocess is delayed, and oil-well construction costs increasesignificantly due to severe shale hydration, swelling, and dispersion.Therefore, many drilling fluids include shale inhibiting agents.

The most widely employed shale inhibiting agent is potassium chloride.Additives, such as polyacrylamide, polyglycol, and silicates, may becombined with the potassium chloride to obtain better characteristics.Massive quantities of potassium chloride are required for achieving thedesired shale inhibition, resulting in contamination and environmentalissues due to the introduction of a large concentration of chlorideions. Other shale inhibiting materials include amine- and imine-basedlow or high molecular weight compounds, acrylamides, glycols, glycerols,biomolecules, formate salts, silicates, and the like. Due to variablecharacteristics, such as the irregular shape of clay minerals, a widevariation in the particle size, various types of charges, the ionexchange capacity, and the flexibility of the layers, no shale inhibitorcompounds have been entirely successful in stabilizing the borehole.

SUMMARY

Therefore, there is a continual need for a water-based shale inhibitorthat provides improved borehole stability. Embodiments of the presentdisclosure are directed to cationic polymers, and methods of using forinhibiting shale formation during water-based drilling of subterraneanformations while achieving improved borehole stability.

According to an embodiment, a method of inhibiting shale formationduring water-based drilling of subterranean formations includesintroducing a shale inhibitor to the subterranean formation during thewater-based drilling, the shale inhibitor comprising a cationic polymercomprising repeating units of [A-B]. A is a substituted benzene or asubstituted triazine of formula (2):

A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N. R¹, R², R³, R⁴, R⁵,and R⁶ are independently a bond to B of formula (1), a hydrogen radical,X, an unsubstituted alkyl, or an alkyl bearing at least one substituentX. X is independently Cl, Br, or I. B is a N-containing heterocycle.

According to an embodiment, a method of making the cationic polymer, asdefined above, includes introducing a substituted benzene or asubstituted triazine of formula (2) to a N-containing heterocycle toobtain a reaction mixture having a molar ratio of the substitutedbenzene or the substituted triazine of formula (2) to the N-containingheterocycle, and maintaining the reaction mixture in a solvent at atemperature from 0° C. to 50° C. for from 2 hours to 24 hours.

According to an embodiment, a cationic polymer comprises repeating unitsof [A-B], as defined above.

Additional features and advantages of the embodiments described hereinwill be set forth in the detailed description which follows, and in partwill be readily apparent to those skilled in the art from thatdescription or recognized by practicing the embodiments described,including the detailed description and the claims which are providedinfra.

DETAILED DESCRIPTION

As used herein, the term “hydrocarbon” refers to a chemical compoundcomprising carbon and hydrogen atoms. An expression such as “C_(X)-C_(y)hydrocarbon” refers to a hydrocarbon having from x to y carbon atoms.For instance, a C₁-C₅ hydrocarbon includes methane, ethane, propane,butane, isobutane, pentane, isopentane, and neopentane. Other atoms mayalso be present, such as oxygen, sulfur, and nitrogen, for example.

As used herein, the term “subterranean formation” refers to a depositreservoir that contains a subsurface pool of hydrocarbons contained inporous or fractured rock formations.

As used herein, the term “alkyl” refers to saturated, straight-, orbranched-chain hydrocarbon radicals derived from an aliphatic moietycontaining between one and twenty carbon atoms by removal of a singlehydrogen atom. Unless otherwise specified, alkyl groups contain 1-12carbon atoms. In certain embodiments, alkyl groups contain 1-8 carbonatoms. In embodiments, alkyl groups contain from 1 to 6 carbon atoms. Inembodiments, alkyl groups contain from 1 to 5 carbon atoms. Inembodiments, alkyl groups contain from 1 to 4 carbon atoms. In otherembodiments, alkyl groups contain from 1 to 3 carbon atoms. Inembodiments, alkyl groups contain from 1 to 2 carbon atoms. Exemplaryalkyl radicals include, but are not limited to, methyl, ethyl, n-propyl,isopropyl, n-butyl, isobutyl, sec-butyl, sec-pentyl, isopentyl,tert-butyl, n-pentyl, neopentyl, n-hexyl, sec-hexyl, n-heptyl, n-octyl,n-decyl, n-undecyl, dodecyl, and the like.

As used herein, the term “heterocycle” or “heterocyclic compound” refersto a cyclic compound that has atoms of at least two different elements,such as carbon and nitrogen, as members of the cyclic system.

As used herein, the term “weight-average molecular weight” refers to aproperty of a sample of polymers that is calculated based on the size ofthe individual polymer molecules in a sample, as opposed to“number-average molecular weight,” which is calculated based on thenumber of repeating units in the polymer. Weight-average molecularweight may be given by equation (1):

$\begin{matrix}{M_{w} = \frac{\sum{N_{x}M_{x}^{2}}}{\sum{N_{x}M_{x}}}} & (1)\end{matrix}$

where M_(w) is the weight-average molecular weight, N_(X) is the totalnumber of molecules of length x, and M_(x) is the molecular weight of amolecule corresponding to a degree of polymerization x.

As used herein, the term “thermal stability” of a sample of polymersrefers to the sample's resistance to degradation in the presence of anelevated temperature over a period of time.

Embodiments of the present disclosure are directed toward a method ofinhibiting shale formation during water-based drilling of subterraneanformations. The method includes introducing a shale inhibitor to thesubterranean formation during the water-based drilling. The shaleinhibitor includes a cationic polymer comprising repeating units offormula (1):

[A-B]  (1)

where A is a substituted benzene or a substituted triazine of formula(2).

A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N. R¹, R², R³, R⁴, R⁵,and R⁶ are independently a bond to B of formula (1), a hydrogen radical,X, an unsubstituted alkyl, or an alkyl bearing at least one substituentX. X is independently Cl, Br, or I. B of formula (1) is a N-containingheterocycle. Embodiments described herein are also directed to thecationic polymer comprising repeating units of formula (1).

In embodiments, A of formula (1) is a substituted benzene or asubstituted triazine of formula (2). For example, A may be selected froma triazine compound of formula (3), a benzene compound of formula (4), abenzene compound of formula (5), and a combination of two or more ofthese.

In embodiments, at least one of R¹, R³, and R⁵ is X and the others ofR¹, R³, and R⁵ are a bond to B. In embodiments, R¹ and R⁴ are both bondsto B.

B of formula (1) is a N-containing heterocycle. In embodiments, B is asubstituted or unsubstituted bipyridine, a bridged bicyclic compound offormula (6), a bridged tricyclic compound of formula (7), a pyrazinecompound of formula (8), or a combination of two or more of these.

R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³, and R¹⁴ may be independently an electronpair or a bond to A, wherein if the R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³, orR¹⁴ is a bond to A, the N bears a +1 formal charge. R¹⁵, R¹⁶, R¹⁷, andR¹⁸ are independently a hydrogen radical, hydroxyl, straight or branchedalkyl (such as methyl, ethyl, and propyl), thiol, azide, nitrile, oraryl.

In embodiments in which B is a bipyridine, the bipyridine may be one ormore of the six regioisomers of bipyridine, formulae (9)-(14). Thenitrogen radicals of formulae (9)-(14) are bonded to A and bear a +1formal charge. Each carbon radical of formulae (9)-(14) mayindependently be bonded to a hydrogen radical (and thus beunsubstituted) or may be substituted by being bonded to hydroxyl,straight or branched alkyl (such as methyl, ethyl, and propyl), thiol,azide, nitrile, or aryl.

In embodiments, the cationic polymer of formula (1) may includerepeating units of formula (15), repeating units of formula (16), or acombination of repeating units of formula (15) and formula (16). Ofcourse, the repeating units may be composed of any of the compounds of Adescribed herein and any of the compounds of B described herein.

In embodiments, the cationic polymer of formula (1) may have aweight-average molecular weight M_(w) from 10 kilodaltons (kDa) to 1000kDa, from 20 kDa to 750 kDa, from 25 kDa to 500 kDa, from 75 kDa to 500kDa, or even from 25 kDa to 100 kDa. It should be understood that theweight-average molecular weight M_(w) may be from any lower bound ofsuch weight-average molecular weight described herein to any upper boundof such weight-average molecular weight described herein.

In embodiments, the cationic polymer of formula (1) may have a thermalstability in inert or oxidative atmosphere from 150° C. to 250° C., from175° C. to 225° C., or even from 190° C. to 200° C. In general, a higherthermal stability of the cationic polymer, the less likely the polymeris to degrade at the conditions in a typical wellbore.

In embodiments, the cationic polymer of formula (1) may be associatedwith one or more counter anions. Exemplary counter anions include, butare not limited to, chloride, bromide, iodide, hydroxide, and acombination of two or more of these. Formulae (15) and (16) are shownbearing chloride counter anions, but it is envisioned that anyappropriate counter anion may replace one or more, including all, of thechloride anions shown.

In embodiments, the cationic polymer may be made by introducing asubstituted benzene or a substituted triazine of formula (2) to aN-containing heterocycle to obtain a reaction mixture and maintainingthe reaction mixture in a solvent at a temperature from 0° C. to 50° C.,from 2° C. to 40° C., or even from 25° C. to 35° C., for from 2 hours to24 hours, from 4 hours to 10 hours, or even from 5 hours to 7 hours.

A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N. R¹, R², R³, R⁴, R⁵,and R⁶ are independently a bond to the N-containing heterocycle, X, anunsubstituted alkyl, or an alkyl bearing at least one substituent X. Xis independently Cl, Br, or I. An exemplary substituted benzene orsubstituted triazine of formula (2) includes, but is not limited to,cyanuric chloride, cyanuric bromide, cyanuric iodide,1,3,5-trichlorobenzene, 1,3,5-tribromobenzene, 1,3,5-triiodobenzene,1,3-dibromo-5-chlorobenzene, 1,3-dibromo-5-iodobenzene,1,3-dichloro-5-iodobenzene, 1-chloro-3,5-diiodobenzene,1-bromo-3,5-diiodobenzene, 1-bromo-3,5-dichlorobenzene,1,3,5-tri(chloromethyl)benzene, 1,3,5-tri(bromomethyl)benzene,1,3,5-tri(iodomethyl)benzene, 1,3-dichloromethyl-5-iodomethylbenzene,1,3-dibromomethyl-5-chloromethylbenzene,1,3-dibromomethyl-5-iodomethylbenzene,1-bromomethyl-3,5-dichloromethylbenzene,1-bromomethyl-3,5-diiodomethylbenzene,1-chloromethyl-3,5-diiodomethylbenzene, 1,4-dichlorobenzene,1,4-dibromobenzene, 1,4-diiodobenzene, 1-bromo-4-iodobenzene,1-bromo-4-chlorobenzene, 1-chloro-4-iodobenzene,1,4-di(chloromethyl)benzene, 1,4-di(bromomethyl)benzene,1,4-di(iodomethyl)benzene, 1-bromomethyl-4-chloromethylbenzene,1-bromomethyl-4-iodomethylbenzene, and1-chloromethyl-4-bromomethylbenzene.

In embodiments, the ratio of the substituted benzene or the substitutedtriazine of formula (2) to the N-containing heterocycle may be from 1:05to 1:1.5, from 1:0.2 to 1:1.2, from 1:0.5 to 1:1.1, or even from 1:0.75to 1:1.

In embodiments, the N-containing heterocycle may be a substituted orunsubstituted bipyridine, a compound of formula (6), a compound offormula (7), a compound of formula (8), or a combination of two or moreof these.

R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³ and R¹⁴ are independently an electronpair or a bond to the substituted benzene or a substituted triazine offormula (2), wherein if the R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³, or R¹⁴ is abond to the substituted benzene or a substituted triazine of formula(2), the N bears a +1 formal charge. R¹⁵, R¹⁶, R¹⁷, and R¹⁸ areindependently a hydrogen radical, hydroxyl, straight or branched alkyl(such as methyl, ethyl, and propyl), thiol, azide, nitrile, or aryl. Anexemplary N-containing heterocycle includes, but is not limited to,hexamethylenetetramine, and 1,4-diazabicyclo[2.2.2]octane,6-methyl-2-pyrazinethiol, 5-methyl-2-pyrazinecarbonitrile,2-methyl-5-phenylpyrazine, 2-azido-5-methylpyrazine, and pyrazine.

In embodiments in which the N-containing heterocycle is a bipyridine,the bipyridine may be one or more of the six regioisomers of bipyridine,formulae (9)-(14). The nitrogen radicals of formulae (9)-(14) are bondedto A and bear a +1 formal charge or, at the termini of the polymerchains, bear an electron pair. Each carbon radical of formulae (9)-(14)may independently be bonded to a hydrogen radical (and thus beunsubstituted) or may be substituted by being bonded to hydroxyl,straight or branched alkyl (such as methyl, ethyl, and propyl), thiol,azide, nitrile, or aryl.

In embodiments, the cationic polymer may include repeating units offormula (15), repeating units of formula (16), or a combination ofrepeating units of formula (15) and formula (16). Of course, therepeating units may be composed of any of the substituted benzenes orsubstituted triazines of formula (2) described herein and anyN-containing heterocycle described herein. In embodiments, the cationicpolymer may be associated with one or more counter anions. Exemplarycounter anions include, but are not limited to, chloride, bromide,iodide, hydroxide, and a combination of two or more of these. Formulae(15) and (16) are shown bearing chloride counter anions, but it isenvisioned that any appropriate counter anion may replace one or more,including all, of the chloride anions shown.

In embodiments, the solvent may be one or more of acetonitrile, diethylether, tetrahydrofuran, dioxane, an alcoholic solvent, a chlorinatedsolvent, or an aromatic hydrocarbon solvent. Exemplary alcoholicsolvents include, but are not limited to, methanol, ethanol,isopropanol, t-butanol, pentanol, and mixtures of two or more thereof.Exemplary chlorinated solvents include, but are not limited to, methylchloride, dichloromethane, chloroform, carbon tetrachloride, andmixtures of two or more thereof. Exemplary aromatic hydrocarbon solventsinclude, but are not limited to, benzene, toluene, ortho-xylene,meta-xylene, para-xylene, and mixtures of two or more thereof. Inembodiments, the solvent comprises dichloromethane. In embodiments, thesolvent comprises tetrahydrofuran. In embodiments, both the substitutedbenzenes or substituted triazines of formula (2) and the N-containingheterocycle may be mixed together, and the resulting mixture may then bedissolved in the solvent. In other embodiments, the substituted benzenesor substituted triazines of formula (2) may be dissolved in a solvent,the N-containing heterocycle may be dissolved in the same or a differentsolvent, and then the two resulting solutions may be combined.

In embodiments, the weight of the substituted benzene or the substitutedtriazine of formula (2) and the weight of the N-containing heterocyclemay be added together to provide a total monomer weight. The ratio ofthe total monomer weight to the volume of the solvent may be from 2grams of total monomer per 100 milliliters of solvent (2 g/100 ml) to 50g/100 ml, from 2 g/100 ml to 45 g/100 ml, from 2 g/100 ml to 40 g/100ml, from 2 g/100 ml to 35 g/100 ml, from 2 g/100 ml to 30 g/100 ml, from2 g/100 ml to 25 g/100 ml, from 2 g/100 ml to 20 g/100 ml, from 2 g/100ml to 15 g/100 ml, from 2 g/100 ml to 10 g/100 ml, from 2 g/100 ml to 5g/100 ml, from 5 g/100 ml to 50 g/100 ml, from 5 g/100 ml to 25 g/100ml, from 10 g/100 ml to 50 g/100 ml, from 10 g/100 ml to 15 g/100 ml,from 15 g/100 ml to 50 g/100 ml, from 20 g/100 ml to 50 g/100 ml, from25 g/100 ml to 50 g/100 ml, from 30 g/100 ml to 50 g/100 ml, from 35g/100 ml to 50 g/100 ml, from 40 g/100 ml to 50 g/100 ml, or even from45 g/100 ml to 50 g/100 ml. It should be understood that the ratio ofthe total monomer weight to the volume of the solvent may be in a rangefrom any lower limit of such a ratio described herein to any upper limitof such a ratio described herein.

In embodiments, the temperature may be maintained for a time and thenincreased to an elevated temperature for an additional amount of time.For instance, the reaction mixture may be maintained at a temperaturefrom 0° C. to 12° C. for from 1 hour to 2 hours. Then, the temperaturemay be increased to a range from 12° C. to 50° C.

According to an aspect, either alone or in combination with any otheraspect, a method of inhibiting shale formation during water-baseddrilling of subterranean formations includes introducing a shaleinhibitor to the subterranean formation during the water-based drilling,the shale inhibitor comprising a cationic polymer comprising repeatingunits of [A-B]. A is a substituted benzene or a substituted triazine offormula (2):

A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N. R¹, R², R³, R⁴, R⁵,and R⁶ are independently a bond to B of formula (1), a hydrogen radical,X, an unsubstituted alkyl, or an alkyl bearing at least one substituentX. X is independently Cl, Br, or I. B is a N-containing heterocycle.

According to a second aspect, either alone or in combination with anyother aspect, A is selected from the group consisting of:

and a combination of two or more thereof.

According to a third aspect, either alone or in combination with anyother aspect, at least one of R¹, R³, and R⁵ is X and the others of R¹,R³, and R⁵ are a bond to B.

According to a fourth aspect, either alone or in combination with anyother aspect, R¹ and R⁴ are both bonds to B.

According to a fifth aspect, either alone or in combination with anyother aspect, B is selected from the group consisting of:

a substituted or unsubstituted bipyridine, and a combination of two ormore thereof. R⁷, R⁸, R⁹, r¹⁰, r¹¹, R¹², R¹³, and R¹⁴ are independentlyan electron pair or a bond to A, wherein if the R⁷, R⁸, R⁹, R¹⁰, R¹¹,R¹², R¹³, or R¹⁴ is a bond to A, the N bears a +1 formal charge. R¹⁵,R¹⁶, R¹⁷, and R¹⁸ are independently a hydrogen radical, hydroxyl,straight or branched alkyl, thiol, azide, nitrile, or aryl.

According to a sixth aspect, either alone or in combination with anyother aspect, the cationic polymer comprises repeating units of formula(15), repeating units of formula (16), or a combination of repeatingunits of formula (15) and formula (16):

According to a seventh aspect, either alone or in combination with anyother aspect, the cationic polymer has a weight-average molecular weightfrom 10 kilodaltons (kDa) to 1000 kDa.

According to an eighth aspect, either alone or in combination with anyother aspect, the cationic polymer has a weight-average molecular weightfrom 25 kilodaltons (kDa) to 500 kDa.

According to a ninth aspect, either alone or in combination with anyother aspect, the cationic polymer has a weight-average molecular weightfrom 25 kilodaltons (kDa) to 100 kDa.

According to a tenth aspect, either alone or in combination with anyother aspect, a method of making a cationic polymer introducing asubstituted benzene or the substituted triazine of formula (2) to aN-containing heterocycle to obtain a reaction mixture having a molarratio of the substituted benzene or the substituted triazine of formula(2) to the N-containing heterocycle.

According to an eleventh aspect, either alone or in combination with anyother aspect, the ratio of the substituted benzene or the substitutedtriazine of formula (2) to the N-containing heterocycle is from 1:0.2 to1:1.2.

According to a twelfth aspect, either alone or in combination with anyother aspect, the solvent is selected from the group consisting oftetrahydrofuran, dioxane, an alcoholic solvent, a chlorinated solvent,an aromatic hydrocarbon solvent, and a mixture of two or more of these.

According to a thirteenth aspect, either alone or in combination withany other aspect, the solvent is selected from the group consisting ofmethanol, ethanol, isopropanol, t-butanol, pentanol, and a mixture oftwo or more of these.

According to a fourteenth aspect, either alone or in combination withany other aspect, the solvent is selected from the group consisting ofmethyl chloride, dichloromethane, chloroform, carbon tetrachloride, anda mixture of two or more of these.

According to a fifteenth aspect, either alone or in combination with anyother aspect, the solvent is selected from the group consisting ofbenzene, toluene, ortho-xylene, meta-xylene, para-xylene, and a mixtureof two or more of these.

According to a sixteenth aspect, either alone or in combination with anyother aspect, the substituted benzene or the substituted triazine offormula (2) and the N-containing heterocycle have a total monomerweight, the solvent has a solvent volume, and a ratio of the totalmonomer weight to the solvent volume is from 2 g/100 ml to 50 g/100 ml.

According to a seventeenth aspect, either alone or in combination withany other aspect, the reaction mixture in a solvent is maintained at atemperature from 0° C. to 12° C. for from 1 hour to 2 hours and then thetemperature is increased in a range from 12° C. to 50° C.

According to an eighteenth aspect, either alone or in combination withany other aspect, a cationic polymer includes repeating units of [A-B],where A and B are defined as above.

Examples

Using embodiments described above, exemplary cationic polymers weresynthesized and used to study their effectiveness as shale inhibitingagents. The following examples are merely illustrative and should not beinterpreted as limiting the scope of the present disclosure.

Synthesis of Cationic Heterocyclic Polymers:

Synthesis of Polymer POLY A+(Formula (15)):

The molar ratio of a mixture of cyanuric chloride andhexamethylenetetramine was maintained at 1:0.5. In a reaction vessel,hexamethylenetetramine (14 g, 0.1 mol) was dissolved in 500 mltetrahydrofuran at room temperature, and the solution was cooled to 0°C. Cyanuric chloride (36.8 g, 0.2 mol) was dissolved in 100 mltetrahydrofuran in a separate vessel. The cyanuric chloride solution wasadded to the hexamethylenetetramine solution with stirring over 30minutes. The reaction temperature was maintained at 0° C. to 5° C. forone hour. Subsequently, the reaction mixture was heated to roomtemperature (25° C. to 30° C.) and stirred at this temperature for fiveto six hours, resulting in the formation of a precipitate. Theprecipitate thus formed was filtered and dried at 80° C. to 100° C. forfive hours in a vacuum oven.

Synthesis of Polymer POLY B+(Formula (16)):

The molar ratio of cyanuric chloride and 1,4-Diazabicyclo[2.2.2]octane(DABCO) was maintained at 1:1. In a reaction vessel, DABCO (11.2 g, 0.1mol) was mixed with 200 ml tetrahydrofuran at room temperature, and thesolution was cooled to 0° C. Cyanuric chloride (18.4 g, 0.1 mol) wasdissolved in 50 ml tetrahydrofuran in a separate vessel. The cyanuricchloride solution was added to the DABCO solution with stirring over 30min. The reaction temperature was maintained at 0° C. to 5° C. for onehour. Subsequently, the reaction mixture was heated to room temperature(25° C. to 30° C.) and stirred at this temperature for five to sixhours, resulting in the formation of a precipitate. The precipitate thusformed was filtered and dried at 80° C. to 100° C. for five hours in avacuum oven.

Clay Swelling Test:

To observe the effects of POLY A+ and POLY B+ on swelling in claymaterials, a clay swelling test was performed using a Fann CapillarySuction Timer (CST). To perform the clay swelling test, formulationswere prepared in accordance with Table 1. Each formulation (5 ml) wasused for the CST experiments, and the rate of water passing throughfilter paper via capillary suction using the CST was recorded.

TABLE 1 Clay swelling test formulations and results Component C1 I1 I2C2 C3 C4 Water (g) 250 250 250 250 250 250 Bentonite (g) 5.1 5.1 5.1 5.15.1 5.1 Silica flour (g) 24.9 24.9 24.9 24.9 24.9 24.9 Poly A+ (g) — 2.5— — — — Poly B+ (g) — — 2.5 — — — Choline chloride (g) — — — 2.5 — — KCl— — — — 2.5 — Hexamethylene diamine — — — — — 2.5 (HIPERM ™) (g)Normalized Time (s) 400.2 12.5 12.1 13.3 13.9 13.6

As shown above, the formulations including POLY A+ and POLY B+ exhibitedfaster rates of water passing through filter paper via capillary suctionusing the CST compared with the comparative formulations C1-C4. As aresult, the formulations including POLY A+ and POLY B+ have a superiorperformance relative to the comparative formulations. Without intendingto be bound by any particular theory, it is believed that clay swellinginhibitors or shale inhibitors used in wellbore fluids and otherwellbore construction and production applications may be utilized to atleast partially prevent clay-based materials from swelling duringwellbore construction and production enhancement operations. Further, itis believed that a faster normalized time suggests that the clays arenot retaining as much water, thereby minimizing water interaction withthe clays. Therefore, the results obtained above suggest that theformulations including POLY A+ and POLY B+ exhibit superior swellretarding effects when compared to the comparative examples.

Shale Dispersion Test:

Pierre II Shale, which has the composition provided in Table 2, was usedin the shale dispersion test. Shale cuttings were broken into smallpieces with a benchtop jaw crusher or manually, with a hammer, andpassed through a #4 mesh screen having openings of 4760 μm (0.187inches). The shale material that passed through the #4 mesh screen wasthen passed over a #8 mesh screen having openings of 2380 μm (0.0937inches). The material that passed through the #8 mesh screen wasdisposed of, while the material that could not pass through the screenwas saved for shale erosion studies.

TABLE 2 Composition of Piere II Shale Component Weight percent (%)Quartz 36 Potassium feldspar 4 Plagioclase 6 Calcite 1 Dolomite 5 Pyrite2 Chlorite 3 Kaolinite 1 Smectite 24 Illite 18

Shale dispersion tests were performed using two types of base fluids:synthetic Arabian Sea water and de-ionized water. The synthetic ArabianSea water included: CaCl₂) (1.71 g/l), MgCl₂ (8.26 g/l), KCl (1.13 g/l),NaCl (41.72 g/l), NaHCO₃ (0.21 g/l), and Na₂SO₄ (6.12 g/l). Samples wereprepared using inhibitors, xanthan gum, and synthetic Arabian Sea water(Table 3) or de-ionized water (Table 4) in amounts provided by Tables 3and 4. The xanthan gum was used as a viscosifier for better suspendingthe relatively large Pierre II shales. Other viscosifiers that could beused include, but are not limited to, partially hydrolyzedpolyacrylamide, acrylic acid, hydroxylated ethyl cellulose, and acombination of any two or more of these. Pierre II shales prepared asabove were then added into the fluids and the dispersion was hot rolledat 26.7° C. (80° F.) for 16 hours. After 16, hours, the dispersion waspassed through a #8 mesh screen having openings of 2380 μm (0.0937inches) to recover shales that were not swelled.

TABLE 3 Formulations and shale stability in synthetic Arabian SeaComponent C5 C6 C7 C8 I3 I4 Synthetic Arabian Sea water (g) 58.3 58.358.3 58.3 250 58.3 Xanthan gum (g) 0.125 0.125 0.125 0.125 0.125 0.125Pierre II shale (g) 5 5 5 5 5 5 Choline chloride (g) — 0.5 — — — — KCl(g in 20 g water) — — 0.5 — — — Hexamethylene diamine — — — 0.5 — —(HIPERM ™) (g in 20 g water) Poly A+ (g in 20 g water) — — — — 0.5  Poly B+ (g in 20 g water) — — — — — 0.5 Shale recovered (%) 63.8 81.675.4 72.2 84.4 87.6

TABLE 4 Formulations and shale stability in de-ionized water ComponentC5 C6 C7 C8 I3 I4 De-ionized water (g) 58.3 58.3 58.3 58.3 250 58.3Xanthan gum (g) 0.125 0.125 0.125 0.125 0.125 0.125 Pierre II shale (g)5 5 5 5 5 5 Choline chloride (g) — 0.5 — — — — KCl (g in 20 g water) — —0.5 — — — Hexamethylene diamine — — — 0.5 — — (HIPERM ™) (g in 20 gwater) Poly A+ (g in 20 g water) — — — — 0.5   Poly B+ (g in 20 g water)— — — — — 0.5 Shale recovered (%) 0.4 57.9 50.3 53.4 59.1 50.4

The amount of recovered shales after shale dispersion tests werecalculated from weight loss after the test, and are presented in Table 3(synthetic Arabian Sea water) and Table 4 (de-ionized water). The shaledispersion studies demonstrate the higher recovery of shales wheninhibitors were employed in the shale dispersion test. Furthermore, theshales treated with POLY A+ and POLY B+ gave higher recovery of shalescompared to traditional shale inhibitors, choline chloride, KCl, andhexamethylene diamine, as well as compared to the experiment withoutinhibitor. The shale stability test in de-ionized water showedsubstantial loss of shales compared to the test in synthetic Arabian Seawater, which corresponds to a higher swelling in fresh water compared tosynthetic Arabian Sea water. A higher amount of salts in the sea watercould also contribute in the shale inhibition characteristic. The testalso suggests that all the shales were swollen when there was noinhibitor added in the de-ionized water experiment; the amount of shalerecovered was only 0.4%.

It is noted that recitations in the present disclosure of a component ofthe present disclosure being “operable” or “sufficient” in a particularway, to embody a particular property, or to function in a particularmanner, are structural recitations, as opposed to recitations ofintended use. More specifically, the references in the presentdisclosure to the manner in which a component is “operable” or“sufficient” denotes an existing physical condition of the componentand, as such, is to be taken as a definite recitation of the structuralcharacteristics of the component.

Having described the subject matter of the present disclosure in detailand by reference to specific embodiments, it is noted that the variousdetails disclosed in the present disclosure should not be taken to implythat these details relate to elements that are essential components ofthe various embodiments described in the present disclosure. Further, itwill be apparent that modifications and variations are possible withoutdeparting from the scope of the present disclosure, including, but notlimited to, embodiments defined in the appended claims.

The singular forms “a,” “an,” and “the” include plural referents, unlessthe context clearly dictates otherwise.

Throughout this disclosure ranges are provided. It is envisioned thateach discrete value encompassed by the ranges are also included.Additionally, the ranges which may be formed by each discrete valueencompassed by the explicitly disclosed ranges are equally envisioned.

As used in this disclosure and in the appended claims, the words“comprise,” “has,” and “include,” and all grammatical variations thereofare each intended to have an open, non-limiting meaning that does notexclude additional elements or steps.

As used in this disclosure, terms such as “first” and “second” arearbitrarily assigned and are merely intended to differentiate betweentwo or more instances or components. It is to be understood that thewords “first” and “second” serve no other purpose and are not part ofthe name or description of the component, nor do they necessarily definea relative location, position, or order of the component. Furthermore,it is to be understood that the mere use of the term “first” and“second” does not require that there be any “third” component, althoughthat possibility is contemplated under the scope of the presentdisclosure.

What is claimed is:
 1. A method of making a cationic polymer, comprisingintroducing a substituted benzene or a substituted triazine of formula(2) to a N-containing heterocycle to obtain a reaction mixture having amolar ratio of the substituted benzene or the substituted triazine offormula (2) to the N-containing heterocycle:

where A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N; R¹, R², R³,R⁴, R⁵, and R⁶ are independently a bond to the N-containing heterocycle,a hydrogen radical, X, an unsubstituted alkyl, or an alkyl bearing atleast one substituent X; X is independently Cl, Br, or I; and at leastone of R¹, R³, and R⁵ is X and the others of R¹, R³, and R⁵ are a bondto the N-containing heterocycle; and maintaining the reaction mixture ina solvent at a temperature from 0° C. to 50° C. for from 2 hours to 24hours.
 2. The method of claim 1, wherein the ratio of the substitutedbenzene or the substituted triazine of formula (2) to the N-containingheterocycle is from 1:0.2 to 1:1.2.
 3. The method of claim 1, whereinthe solvent is selected from the group consisting of tetrahydrofuran,dioxane, an alcoholic solvent, a chlorinated solvent, an aromatichydrocarbon solvent, and a mixture of two or more of these.
 4. Themethod of claim 3, wherein the solvent is selected from the groupconsisting of methanol, ethanol, isopropanol, t-butanol, pentanol, and amixture of two or more of these.
 5. The method of claim 3, wherein thesolvent is selected from the group consisting of methyl chloride,dichloromethane, chloroform, carbon tetrachloride, and a mixture of twoor more of these.
 6. The method of claim 3, wherein the solvent isselected from the group consisting of benzene, toluene, ortho-xylene,meta-xylene, para-xylene, and a mixture of two or more of these.
 7. Themethod of claim 1, wherein the substituted benzene or the substitutedtriazine of formula (2) and the N-containing heterocycle have a totalmonomer weight, the solvent has a solvent volume, and a ratio of thetotal monomer weight to the solvent volume is from 2 g/100 ml to 50g/100 ml.
 8. The method of claim 1, wherein the reaction mixture in asolvent is maintained at a temperature from 0° C. to 12° C. for from 1hour to 2 hours and then the temperature is increased in a range from12° C. to 50° C.
 9. The method of claim 1, wherein the cationic polymercomprises repeating units of formula (15), repeating units of formula(16), or a combination of repeating units of formula (15) and formula(16):


10. A cationic polymer comprising repeating units of formula (1):[A-B]  (1) where A is a substituted benzene or a substituted triazine offormula (2):

where A¹, A², A³, A⁴, A⁵, and A⁶ are independently C or N; R¹, R², R³,R⁴, R⁵, and R⁶ are independently a bond to B of formula (1), a hydrogenradical, X, an unsubstituted alkyl, or an alkyl bearing at least onesubstituent X; X is independently Cl, Br, or I; and at least one of R¹,R³, and R⁵ is X and the others of R¹, R³, and R⁵ are a bond to B; and Bis a N-containing heterocycle.
 11. The cationic polymer of claim 10,wherein the cationic polymer comprises repeating units of formula (15),repeating units of formula (16), or a combination of repeating units offormula (15) and formula (16):


12. The cationic polymer of claim 10, wherein A is selected from thegroup consisting of:

and a combination thereof.
 13. The cationic polymer of claim 10, whereinB is selected from the group consisting of:

a substituted or unsubstituted bipyridine, and a combination of two ormore thereof, where R⁷, R⁸, R⁹, R¹⁰, R¹², R¹³, and R¹⁴ are independentlyan electron pair or a bond to A, wherein if the R⁷, R⁸, R⁹, R¹⁰, R¹¹,R¹², R¹³, or R¹⁴ is a bond to A, the N bears a +1 formal charge; andR¹⁵, R¹⁶, R¹⁷, and R¹⁸ are independently a hydrogen radical, hydroxyl,straight or branched alkyl, thiol, azide, nitrile, or aryl.
 14. Thecationic polymer of claim 10, wherein the cationic polymer has aweight-average molecular weight from 10 kilodaltons (kDa) to 1000 kDa.15. The cationic polymer of claim 10, wherein the cationic polymer has aweight-average molecular weight from 25 kilodaltons (kDa) to 500 kDa.16. The cationic polymer of claim 10, wherein the cationic polymer has aweight-average molecular weight from 25 kilodaltons (kDa) to 100 kDa.